MedTrace Logo

eTMS for Veterans and First Responders With PTSD

NCT06294106 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-08-11

No results posted yet for this study

Summary

A battery of physiological and behavioral data will be collected before and after application of eTMS. Participants will be veterans or first responders diagnosed with PTSD. Study will be a double-blind, sham-controlled, parallel group, randomized clinical trial.

Conditions

  • Post Traumatic Stress Disorder

Interventions

DEVICE

Electroencephalogram personalized Transcranial Magnetic Stimulation (eTMS)

EEG is utilized to determine a personalized frequency to then apply TMS to the frontal lobe.

Sponsors & Collaborators

  • Wave Neuroscience

    collaborator INDUSTRY

  • Virginia Polytechnic Institute and State University

    lead OTHER

Principal Investigators

  • Wynn Legon, PhD · Virginia Polytechnic Institute and State University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-10
Primary Completion
2026-04-30
Completion
2026-04-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06294106 on ClinicalTrials.gov